Business · 01/04/2021Updated: 10/17/2026 · 1 min read
FDA Revokes Emergency Use Authorization for NovaSterilis' Medical Device
Summary
The US Food and Drug Administration (FDA) has revoked the Emergency Use Authorization (EUA) for NovaSterilis' medical device, the Nova2200, which uses the NovaClean decontamination process, citing reasons under the Federal Food, Drug, and Cosmetic Act (FD&C Act).
Original source language: Federal Register — Food and Drug AdministrationOpen original release →